Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Enrique Montoya's research focuses on the clinical presentation and genetic underpinnings of various medical conditions, as indicated by his recent publications. His work includes investigating muscle metastases as the primary manifestation of renal cell carcinoma and identifying novel pathogenic interstitial deletions on chromosome 10q21.1q21.3 associated with neurodevelopmental delay, musculoskeletal disorders, and dysmorphia. Montoya has also contributed to understanding rare genetic conditions, such as a dual diagnosis of Noonan syndrome and hypophosphatasia in an adolescent patient. His scholarship metrics include an h-index of 12, with 31 total publications and 430 citations. Montoya collaborates with Aixa Gonzalez Garcia and T. Burrow at the University of Arkansas for Medical Sciences, with whom he shares one publication each. He remains an active researcher, with his most recent publication in 2025.
Metrics
- h-index: 12
- Publications: 31
- Citations: 430
Selected Publications
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Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3 (2025)
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P179: Never two late: A dual diagnosis of Noonan syndrome and hypophosphatasia in an adolescent patient with unusual presentation (2023)
Collaboration Network
Top Collaborators
- P179: Never two late: A dual diagnosis of Noonan syndrome and hypophosphatasia in an adolescent patient with unusual presentation
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
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